Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J3/00—Processes of treating or compounding macromolecular substances
  • C08J3/12—Powdering or granulating
  • C08J3/122—Pulverisation by spraying
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
  • C08G77/04—Polysiloxanes
  • C08G77/06—Preparatory processes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
  • C08L83/04—Polysiloxanes
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J183/00—Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Adhesives based on derivatives of such polymers
  • C09J183/04—Polysiloxanes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
  • C08G77/04—Polysiloxanes
  • C08G77/12—Polysiloxanes containing silicon bound to hydrogen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
  • C08G77/04—Polysiloxanes
  • C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2383/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
  • C08J2383/04—Polysiloxanes

Definitions

• the present invention relates to substantially silanol-free silicone resin powder having a primary particle size in the range of 0.1-200 nm and an aggregate particle size of 10 nm to 200 microns. More particularly, the present invention relates to a method involving the pretreatment of an organic solvent dispersion of an organosiloxane hydrolyzate with an organosilicon nitrogen material, such as an organosilylamine, or organosilazane, and the spray drying of the resulting mixture to form a substantially silanol-free silicone resin powder useful for making heat curable organopolysiloxane compositions having improved processing characteristics.
• an organosilicon nitrogen material such as an organosilylamine, or organosilazane
• a method for making silicone resin powder is shown by Wolfgruber et al, U.S. Pat. No. 4,935,484.
• An aqueous colloidal suspension of an organo siloxane copolymer is spray dried to produce a silicone resin powder having an average particle diameter of 10 to 150 nm.
• spray dried powders made by Wolfgruber et al can be utilized in a variety of applications as fillers, the powders are contaminated with the emulsifying agent which was was used in the preparation of the organosiloxane copolymer.
• silicone resin powder made by spray drying an aqueous silicone mixture can be used as a substitute for finely divided silica in plastics.
• a free flowing organosilicon resin powder having a primary particle size of 0.1-200 nm and an aggregate particle size of 10 nm to 200 microns.
• useful heat curable silicone compositions such as PSAs can be formulated by spray drying the organic solvent dispersions of the organosiloxane hydrolyzates, the viscosites of the resulting PSAs, or component mixtures used in making the heat curable mixture sometimes exceed optimum processing requirements.
• organosilicon resin powder having a primary particle size in the range of 0.1-200 nm, and an aggregate particle size of 10 nm to 200 microns which would be useful in combining with silicone network ingredients, such as a vinyl substituted organopolysiloxane fluid, a silicon hydride siloxane fluid and platinum catalyst to form a PSA having improved processing characteristics.
• silicone network ingredients such as a vinyl substituted organopolysiloxane fluid, a silicon hydride siloxane fluid and platinum catalyst to form a PSA having improved processing characteristics.
• the present invention is based on the discovery that free flowing substantially silanol-free organosilicon resin powder can be made which is compatible with silicone fluids and useful for making heat curable silicone compositions, such as PSAs.
• a principal feature of the invention is the treatment of an organic solvent dispersion of an organosiloxane hydrolyzate, with sufficient organosilicon nitrogen material, such as an organosilylamine or organosilazane, to render the resulting treated organosiloxane hydrolyzate substantially silanol free, or less than 0.2% by weight of residual hydroxy radicals based on the weight of the organosiloxane hydrolyzate, followed by the spray drying of the resulting organic solvent dispersion.
• the spray dried MQ resin powder which has been treated with the organosilicon nitrogen material can be used directly in combination with silicone network ingredients for making a heat curable silicone composition such as a PSA, as taught by Murakami et al cited above.
• the viscosities of the resulting mixtures have been found to be substantially less as compared to network component mixtures containing untreated spray dried organosiloxane hydrolyzate.
• a method for making free flowing substantially silanol-free silicone resin powder having a primary particle size in the range of 0.1-200 nm and an aggregate particle size of 10 nm to 200 microns which process comprises,
• Radicals included by R in formula (1) are for example C.sub.(1-6) monovalent hydrocarbon radicals and C.sub.(1-6) monovalent hydrocarbon radicals substituted with monovalent radicals inert during condensation or addition reactions.
• monovalent organic radicals such as, C.sub.(1-6) alkyl radicals, for example, methyl, ethyl, propyl, butyl; aryl radicals, such as, phenyl, and halogenated phenyl, for example chlorophenyl.
• the organosiloxane hydrolyzate also can includes M'Q resin comprising benzene soluble organosiloxane comprising Q units as defined in formula (2) chemically combined with M' units selected from a mixture of M units of formula (1) and units selected from the group of,
• R is as previously defined, and R 1 is a C.sub.(2-4) alkenyl radical, and preferably vinyl.
• M' units also can include an average of up to 0 to 25 mole % of diorganodisiloxy units of the formula,
• R 2 is a member selected from the group consisting of R, R 1 and H.
• the organosiloxane hydrolyzate which can be treated with the organosilicon nitrogen material in accordance with the present invention is a toluene dispersible, resinous organosiloxane.
• the organosiloxane can contain from about 0.2% to about 5%, and preferably from about 1% to about 3% by weight of hydroxy radicals based on the total weight of organosiloxane resin.
• a method for making spray dryable organosiloxane hydrolyzate useful in the practice of the invention is by reacting a silica hydrosol, such as a sodium silicate, under acidic conditions with a source of triorganosiloxy units such as shown by formula (1) for example a hexaorganodisiloxane, preferably, hexamethyldisiloxane, or a hydrolyzable triorganosilane, for example, trimethylchlorosilane, or mixtures thereof, followed by recovering a benzene dispersible organosiloxane hydrolyzate.
• a silica hydrosol such as a sodium silicate
• the organosiloxane hydrolyzate can be used as an organic solvent dispersion having 40 to 60% by weight of solids.
• Suitable organic solvents are solvents with boiling points below approximately 250° C. which include suitable aromatic hydrocarbons as well as aliphatic hydrocarbons, such as mineral spirits, hexane, heptane and cyclohexane.
• Spray drying of the organic solvent dispersion of the organosiloxane hydrolyzate can be accomplished in accordance with conventional procedures.
• a spray dryer can be used, for example, having at least one vortex atomizer nozzle with a rotating atomizer in a dry-gas stream or with a two-fluid nozzle.
• the organosiloxane hydrolyzate of the present invention is spray dried from an organic solvent rather than an aqueous colloidal suspension.
• Temperatures which can be employed in the dry-gas stream, such as nitrogen, can be from 90° C. to 300° C. and preferably from 100° C. to 250° C.
• the output temperature of the gas stream formed on drying can be from 50° C. to 200° C.
• the substantially silanol-free organosilicon resin powder of the present invention also can be employed to make damping compositions and potting compositions.
• organosilicon nitrogen materials which can be used in the practice of the invention are organosilylamines or organosilazanes shown by Martellock, U.S. Pat. No. 3,243,404, which is incorporated herein by reference.
• silazanes such as shown in Table 10, p. 186 of An Introduction to the Chemistry of Silicones, by Rochow, 2nd Edition, John Wiley & Sons (1951) also can be used and is incorporated herein by reference.
• hexamethyldisilazane is employed.
• a water/isopropanol/toluene azeotrope was distilled from the solution to provide a 60% by weight of a methylsiloxane hydrolyzate in toluene having a ratio of about 0.65 of trimethylsiloxy units per tetrasiloxy units. It was heated to reflux under nitrogen, and additional water and isopropanol were removed from the toluene dispersion. There was then added 50 parts of hexamethyldisilazane and the reaction mixture was refluxed until IR analysis indicated that the SiOH groups on the methylpolysiloxane resin had been silylated.
• the dispersion of the methylsiloxane hydrolyzate in toluene which had been treated with hexamethyldisilazane was spray dried using a Niro Atomizer portable spray drier type HT equipped with a 2-fluid nozzle with a chamber diameter of 31 inches, a cylindrical height of 2 feet, and a 60 degree conical bottom.
• the inlet/outlet temperatures were 250°/142° C., and the rate was 63 kg/h.
• the product was characterized by FTIR and 29Si NMR which indicated that the silicone resin powder was substantially free of silanol and had a trimethylsiloxy to tetrasiloxy ratio of 0.79.
• Part A There was prepared a mixture of 15 parts of a polydimethylsiloxane having terminal dimethylvinylsiloxy groups and an average of about 20 dimethylsiloxy units, 22.5 parts of the above spray dried methylpolysiloxane resin, 25 ppm of a platinum catalyst as shown by Karstedt, U.S. Pat. No. 3,775,452 and 0.05% based on the weight of mixture of dimethylmaleate as an inhibitor. (Part A)
• Part B There was blended together, 11.14 parts of a polydimethylsiloxane having terminal dimethylhydrogen-siloxy groups and an average of 20.5 dimethylsiloxy units, 0.37 parts of a tetradimethylhydrogensiloxy silicate (a silicon hydride cross-linker) and 17.27 parts of the above spray dried silicone resin powder.
• a pressure sensitive adhesive was prepared by mixing equal molar quantities of the silazane treated Part A and Part B mixtures.
• the silazane treated PSA was applied onto a 1 mil Mylar polyester film at a thickness of about 1.5 mil and cured at 120° C. for 10 minutes.
• the same procedure was followed for preparaing a PSA with the spray dried powder free of silazane.
• the tack and peel adhesion for both PSAs were found to be substantially equivalent.
• the tacks were about 1,000 g/cm 2 and the peel adhesions were about 30 oz/in.

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• Chemical Kinetics & Catalysis (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Silicon Polymers (AREA)
• Adhesives Or Adhesive Processes (AREA)

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• 1993
  • 1993-03-12 US US08/030,740 patent/US5319040A/en not_active Expired - Lifetime
• 1994
  • 1994-02-28 EP EP94301419A patent/EP0614929B1/fr not_active Expired - Lifetime
  • 1994-02-28 DE DE69404876T patent/DE69404876T2/de not_active Expired - Lifetime
  • 1994-03-10 JP JP6038980A patent/JPH06322132A/ja active Pending
• 2006
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